추천 제품
분석
99%
형태
solid
bp
190-192 °C/13 mmHg (lit.)
mp
126-130 °C (lit.)
SMILES string
CC(C)(C)c1ccc(cc1)-c2ccc(cc2)C(C)(C)C
InChI
1S/C20H26/c1-19(2,3)17-11-7-15(8-12-17)16-9-13-18(14-10-16)20(4,5)6/h7-14H,1-6H3
InChI key
CDKCEZNPAYWORX-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
4,4′-Di-tert-butylbiphenyl along with lithium catalyzes:
- reaction of chloromethyl ethyl ether and different carbonyl compounds to yield corresponding hydroxyethers
- reductive opening of N-phenylazetidine
애플리케이션
4,4′-Di-tert-butylbiphenyl was used in production of homoallylic amine derivatives. It was also used in the preparation of lithium di-tert-butylbiphenylide, a radical anion, superior to sodium or lithium naphthalenides for metalation reactions.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
4, 4'-Di -tert -butylbiphenyl-catalysed reductive opening of azetidines with lithium: A direct preparation of 3, N-dilithioalkylamines.
Tetrahedron, 50(19), 5775-5782 (1994)
4, 4′-Di-tert-butylbiphenyl-catalysed lithiation of chloromethyl ethyl ether: A barbier-type new and easy alternative to ethyl lithiomethyl ether.
Tetrahedron Letters, 34(21), 3487-3490 (1993)
The Journal of Organic Chemistry, 55, 1528-1528 (1990)
The Journal of organic chemistry, 66(2), 531-537 (2001-06-30)
Lithiation of the N-2,4,6-triisopropylbenzenesulfonyl-2-pyrroline (16) and treatment of the resulting cyclic vinyllithium reagent with R2CuCNLi2 produced an acyclic vinyl organometallic species that, when treated with an electrophile (H2O or RX), gave the homoallylic sulfonamides 18a-k in 37-93% yields and in
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